Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K3/00—Materials not provided for elsewhere
  • C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
  • C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
  • C09K3/1021—Polyurethanes or derivatives thereof
• • E—FIXED CONSTRUCTIONS
  • E21—EARTH DRILLING; MINING
  • E21D—SHAFTS; TUNNELS; GALLERIES; LARGE UNDERGROUND CHAMBERS
  • E21D11/00—Lining tunnels, galleries or other underground cavities, e.g. large underground chambers; Linings therefor; Making such linings in situ, e.g. by assembling
  • E21D11/38—Waterproofing; Heat insulating; Soundproofing; Electric insulating
  • E21D11/385—Sealing means positioned between adjacent lining members
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G2110/00—Foam properties
  • C08G2110/0041—Foam properties having specified density
  • C08G2110/0066—≥ 150kg/m3
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G2190/00—Compositions for sealing or packing joints

Definitions

• the present invention relates to a water stopping material and a water stopping method using the same. More specifically, a waterproof material that is suitable as a waterproof material in civil engineering, construction and various other fields, is easier to crush than conventional products, and maintains a good airtight waterproofing effect over a long period of time, and a waterproof material is used. It relates to the method of stopping water. Background art
• the sealing material for the tenoned segment that has unevenness on the combined surface of the segments has a lower compressive stress when the segment is constructed. Sealing material is required. This is because the regular segments fix the segments together by fastening the ports, while the tenoned segments fix the segments by combining irregularities, simplifying the method of joining the segments and fastening This is because the force is low and the force to crush the sealing material strongly cannot be expected. It is difficult for a non-foamed water-swellable rubber to meet such a demand for low compressive stress.
• a water-stopping material obtained by foaming a water-swellable rubber is known (for example, Japanese Patent Application Laid-Open No. 57-92032, No. 08-121600, Japanese Patent Application Laid-Open No. 08-157805, Japanese Patent Application Laid-Open No. 09-111899).
• These water-swellable foam waterproofing materials are obtained by kneading a highly water-absorbent resin and a foaming agent into an unvulcanized rubber and vulcanizing and molding.
• the present invention solves the above problems of the conventional water-swellable foamed water-stopping material, has a small mass reduction rate, can maintain the expansion performance due to water absorption over a long period of time, and has a low compression stress water-stopping material and use thereof
• the purpose is to provide a water stoppage method.
• the present invention relates to a water-blocking material comprising a polyurethane foam, wherein the polyurethane foam has a density of 0.3 to 0.9 cm 3 , a volumetric water expansion ratio of 1.2 to 8 times, and 70 in water.
• a oxyethylene group-containing polyurethane foam that has a mass loss rate of 3% or less when immersed in water for 2 days or when immersed in water for 18 days for 180 days, and is made of a molded product or molded product.
• This is a water stopping method using the above-mentioned water stopping material on the combination surface of the segments in the shield d method in which a tunnel is constructed by combining the materials and segments.
• FIG. 1 is a cross-sectional view showing an example of a water-blocking material having a two-layer structure obtained by laminating the oxyethylene group-containing polyurethane foam of the present invention and a porous elastic body.
• FIG. 3 is a perspective view of one embodiment of a segment with a tenon used in the method.
• FIG. 3 is a partial cross-sectional view showing a state in which a tenon (projection) and a tenon (recess) of a tenoned segment are combined to perform sealing.
• Figure 4 shows the adhesion of the steel flange and test piece used to measure the water stop performance.
• FIG. 5 is a conceptual cross-sectional view showing a measurement state of the water stopping performance.
• the water-stopping material of the present invention is a water-stopping material comprising a molded article or a molded article of an oxyethylene group-containing polyurethane foam. It does not contain swelling components that elute, so it has a small mass reduction rate and exhibits stable swelling performance over a long period of time.
• Okishiechiren group-containing polyurethane foam used in the water stopping material of the present invention has a density of usually 0. 3 ⁇ 0. 9 gZcm 3, preferably 0. 45 ⁇ 0. 7 5 gZc m 3 . If the density is less than 0.3 gZcm 3 , the partition walls of the bubbles become thin, and the bubbles are destroyed by the initial compressive stress during segment construction, and good stress relaxation characteristics cannot be obtained. If it exceeds 0.9 gZcm 3 , the effect of reducing the compressive stress during construction of the segment will be reduced.
• Polyurethane foam used in the water stopping material of the present invention in purified water at 2 3, usually from 1.2 to 8 times, preferably a volumetric water swelling ratio when the c having 2-6 times the volume water swelling ratio Is the magnification at which the volume increases due to water absorption, and was determined by the following method. If the volumetric water expansion ratio is less than 1.2 times, the water stopping effect after water expansion cannot be sufficiently obtained, and if it exceeds 8 times, the resin strength after absorbing water and expanding will decrease, so the water stopping performance Can no longer be maintained.
• the content of the oxyethylene group in the polyurethane foam is preferably 5 to 80% by mass, particularly preferably 10 to 60% by mass.
• test piece of 20 x 20 x 2 mm was collected from the polyurethane foam strip, and the volume of this test piece when immersed in purified water of 23: was measured at regular intervals. Calculate the swelling magnification, and use the magnifi- cation when the volume increase per day is 0.01 times or less as the volumetric water swelling magnification of the test specimen.
• volume expansion ratio (times) volume after expansion / volume before expansion
• the mass loss rate is usually 3% by mass or less, preferably 1% by mass or less. is there.
• the mass reduction rate is a measure of the change in mass before and after expansion when immersed in purified water, as is usually done as a method for evaluating the performance of water-swellable sealing materials. It is considered that the components dropped out of the system. The smaller the decrease in mass, the better the durability of the expansion performance.
• the water-swelling component for example, a water-absorbent resin
• the water-stopping material of the present invention that has been increased and that the water-stopping material has been degraded.
• the content of independent air bubbles by the air pycnometer (air-comparison hydrometer) method is usually 60% or more, preferably 8% or more. 0% or more.
• a water-swellable water-stopping material has an effect of giving an airtight waterproof effect by a stress generated by a compressive stress of the water-stopping material at an initial stage of construction. It is not necessary to partially communicate Due to the foam properties, the relaxation of the compressive stress is smaller than that of the conventional water-swellable foam waterproofing material, and there is an advantage that the airtight waterproof effect can be maintained for a longer time.
• the polyurethane foam used for the water-stopping material of the present invention has a compressive stress at a compressibility of 50% of preferably 1 to 25 kgf / cm 2 , particularly preferably 5 to 20 kgf Zcm 2 .
• Airtight waterproof in construction initial compressive stress in the compression rate of 50% is 1 kgf / cm 2 or more is good, when used as a tenon with the segment sealing material When it is 25 kgf / cm 2 or less, water stop Since the pressing force of the segment for crushing the material does not become large, there is no possibility that the assembly accuracy of the segment is adversely affected, and there is no possibility that a crack is generated in the uneven portion of the segment.
• the conventional water-swellable foam waterproofing material expands, and as the absorbed water acts like a plasticizer for the rubber, the rubber softens and the gap between the segments (opening between segments) increases. If the gap is large, a sufficient inflation pressure cannot be obtained.
• the polyurethane foam itself expands, the plasticizing effect due to the absorbed water is small, and the expansion stress is exhibited effectively. Therefore, a better water stopping effect can be obtained.
• the polyurethane foam can be produced by using a foaming agent foaming method, a mechanical floss method and / or a syntactic foam method as a molding method.
• a polyurethane foam can be produced by using either the prepolymer method or the one-shot method using an araliphatic polyisocyanate (b).
• the prepolymer method containing a terminal isocyanate group is preferred because the reactivity in the production of the foam is difficult to control.
• polyoxyalkylene polyol (a 1) containing oxyethylene units examples include polyoxyalkylene ethers of low-molecular-weight active hydrogen-containing compounds having a number average molecular weight of 400 or less as exemplified in the following (1) to (3).
• At least a part of the polyoxyalkylene group is a polyoxyethylene group
• an ethylene oxide (hereinafter abbreviated as E ⁇ ) adduct of this low-molecular-weight active hydrogen-containing compound and Co-adduct with alkylene oxide [C3 or C4 alkylene oxide such as propylene oxide (hereinafter abbreviated as P ⁇ ), butylene oxide, tetrahydrofuran, etc.] (random co-addition) Product or block co-adduct) and the like, and two or more kinds may be used in combination.
• the content of EO is preferred properly 2 0-1 0 0 wt%, more preferably 3 0 to 9 c low molecular weight active hydrogen-containing compound is 0 mass%
• examples include the following.
• Low molecular weight polyols dihydric alcohols such as ethylene glycol, propylene glycol, 1,4- or 1,3-butanediol, diethylene glycol, cyclohexylene diol, and the like; glycerin, trimethylolpropane, and pentaerythris Polyhydric alcohols of 3 to 8 or more, such as tall, sorbitol, and sycrose.
• Polyvalent phenols polyvalent phenols having 2 to 8 or more valences, for example, monocyclic phenols such as hydroquinone, resorcinol, and catechol; bisphenol A, bisphenol B, bisphenol F, bis Bisphenols such as phenol S.
• alkanolamines (monoethanolamine, monobutanolamine, triethanolamine, isopropanolamine, N-methylgenolamine, etc.), alkylamines [alkyl Group carbon number: 2 to 15] (Ethylamine, n-butylamine, octylamine, etc.), alkylene polyamine [Carbonyl group of alkylene: 2 to 6] (Ethylenediamine, hexamethylenediamine, diethylenetriamine, etc.) , Alicyclic diamine [carbon number: 4 to 15] (isophoronediamin, cyclohexylenediamine, etc.), aromatic diamine [carbon number: 6 to 20] (phenylenediamine, diaminotoluene, getyltoluene) Amines, dimethylthiotoluenediamine, xylylenediamine, etc.), heterocyclic polyamines [carbon number: 4 to 15]
• Preferred as (a 1) are polyoxyethylene-polyoxypropylene ethers of low molecular polyols or polyhydric phenols (especially bisphenols) [co-addition of EO and PO (random or block). can get. And a combination thereof, and more preferred are polyoxyethylene-polyoxypropylene ethers of polyvalent phenols. This is because low-molecular-weight polyols such as polyoxyethylene-polyoxypropylene ethers have relatively low reactivity adjustment, and are derived from polyoxyethylene-polypropylene ether, a polyhydric phenol having an aromatic ring. This is because polyurethane foam has good physical properties after water expansion.
• the number average molecular weight of (a 1) is preferably from 600 to 600, more preferably from 100 to 500.
• the average number of functional groups (average number of 10H groups) of (a l) is preferably 2 to 4, more preferably 2 to 3.
• a polyoxyalkylene polyol (a 2) containing no oxyethylene unit is preferably used as the polyol, and the content of the oxyethylene group in the polyurethane foam is preferably 5 to 80% by mass. It may be used in such a range.
• Examples of (a 2) include polyoxyalkylene ethers of low-molecular-weight active hydrogen-containing compounds (1) to (3) (alkylene groups having 3 and Z or 4 carbon atoms), Addition or co-addition of alkylene oxides other than EO [C3 or C4 alkylene oxides, for example, one or more of PO, butylene oxide, tetrahydrofuran, etc.] (if co-added, random Addition or block addition). Of these, preferred are PO adducts of low molecular weight polyols or polyhydric phenols (especially bisphenols) for the same reasons as in (al).
• the number average molecular weight of (a2) is preferably from 600 to 600, more preferably from 100 to 500. Also, the average number of functional groups of (a 2)
• Average number of OH groups is preferably 2 to 4, more preferably 2 to 3.
• Aliphatic, alicyclic or araliphatic polyisocyanates include ethylene diisocyanate, tetramethylene diisocyanate, hexamethylene diisocyanate (HDI), dodecamethylene diisocyanate.
• aliphatic or alicyclic diisocyanates preferred are aliphatic or alicyclic diisocyanates, and particularly preferred are HDI, IPDI and hydrogenated MDI.
• (b) is preferably reacted in a conventional manner at 60 to 150.
• the equivalent of the isocyanate group in (b) to one equivalent of the active hydrogen-containing group in (al) is preferably about 1.2 to 10 or so.
• the content of the isocyanate group in the obtained prepolymer is preferably 2 to 25% by mass, more preferably 4 to 20% by mass.
• (a2) For the purpose of adjusting the content of the oxyethylene group in the polyurethane foam to a preferable range of 5 to 80% by mass, if necessary, (a2) may be used during the production of prepolymer.
• a curing agent such as a chain extender or a cross-linking agent
• a curing agent for example, polyamine (including diamine) among low molecular polyols and low molecular amines exemplified as the low molecular active hydrogen-containing compound used as the raw material of (al) is used. be able to.
• a high molecular compound such as the compounds exemplified as the above (a1) and (a2) may be used as a curing agent, or two or more curing agents may be used in combination.
• a urethanization reaction catalyst (a metal catalyst such as dibutyltin dilaurate, lead octylate, and sodium succinate, an amine catalyst such as triethylamine, triethylenediamine, etc.), a filler, (Talc, bentonite, calcium carbonate, lithobon, silica, my strength, etc.), coloring agents (titanium white, red iron, carbon black, chrome green, etc.), UV absorbers, antioxidants, plasticizers, etc.
• a urethanation reaction can be performed.
• the catalyst is preferably 5% or less, more preferably 0.001 to 3.5%, based on the total mass of all components to obtain the polyurethane foam.
• the filler is preferably 50% or less, more preferably 30% or less.
• the colorant is preferably at most 1%.
• the content of the ultraviolet absorber is preferably 1% or less, and more preferably 0.01% to 0.5%.
• the content of the antioxidant is preferably 1% or less, and more preferably 0.01% to 0.5%.
• the plasticizer is preferably at most 10%, more preferably at most 5%.
• Foaming agents in the foaming method, ordinary foaming agents for polyurethane foam such as water, methylene chloride, halogenated hydrocarbons containing hydrogen atoms (alternative fluorocarbons), low-boiling hydrocarbons, and liquefied carbon dioxide can be used.
• ordinary foaming agents for polyurethane foam such as water, methylene chloride, halogenated hydrocarbons containing hydrogen atoms (alternative fluorocarbons), low-boiling hydrocarbons, and liquefied carbon dioxide can be used.
• halogenated hydrocarbons containing hydrogen atoms alternative fluorocarbons
• low-boiling hydrocarbons low-boiling hydrocarbons
• liquefied carbon dioxide liquefied carbon dioxide
• HC FC Hydrophilicity parameter type (eg, HCF C-123, HC FC-141 b, HCFC-22, and HCF C-142 b)
• HF C Hydrophilic compound type (eg, HF C-134a, HFC-152a, HFC-356m ff, HF C-236 ea, HFC-245 ca, HF C-245 fa And HFC-36 5 mcf)
• the low-boiling hydrocarbon is a hydrocarbon having a boiling point of usually 15 to 7 Ot: and specific examples thereof include butane, pentane, cyclopentane and a mixture thereof.
• Preferred among these is foaming with water.
• water When water is used, it is used in an amount of usually 0.1 to 30%, preferably 1 to 20%, based on the total weight of the polyol used for forming the polyurethane foam.
• the amount used is usually 50% or less, preferably 5 to 45%, based on the total mass of the polyol.
• the amount used is usually 50% or less, preferably 5 to 45%, based on the total weight of the polyols.
• ⁇ Used amount when using low boiling hydrocarbons Is usually 45% or less, preferably 5 to 40%, based on the total mass of the polyol.
• the amount used is usually 30% or less, preferably 5 to 25%, based on the total mass of the polyol.
• the mechanical floss method is a foaming method in which an inert gas such as air or nitrogen is mixed with a raw material mixture for urethanization reaction as described above by a mixing head, and bubbles are mixed. Foaming by mixing nitrogen is preferred.
• the syntactic foam method is a method of forming a foam using hollow microspheres.
• hollow microspheres made of inorganic material [glass bar Runes, silica balloons, etc.), hollow microspheres made of thermosetting resin [phenol resin balloons, epoxy resin balloons, etc.], hollow microspheres made of thermoplastic resin [acrylic resin (polyacrylonitrile) balloons, polyvinylidene chloride balloons] Etc.] can be used.
• it is an acrylic resin balloon.
• a small amount of hollow microspheres may be added as a bubble retaining material.
• the amount of the hollow microspheres used is preferably 60% or less, more preferably 0.2 to 40%, based on the total mass of all components for obtaining a polyurethane foam.
• a foam stabilizer particularly a foam stabilizer that forms closed cells, for stabilizing bubbles.
• an ordinary foam stabilizer for polyurethane foam can be used, and examples thereof include a silicone surfactant such as a polyoxyalkylene-polysiloxane copolymer.
• foam stabilizers that form closed cells include “SZ-1931”, “SZ-1332”, and “SZ-1340” [manufactured by Nippon Rikiichi Co., Ltd. ), "SF-2962", “SF-2965”, “SH-190", “SH-192” (manufactured by Toray Dow Corning Silicone Co., Ltd.), etc. .
• the amount of the foam stabilizer used is preferably 3% or less, more preferably 0.1 to 2%, based on the total mass of all components for obtaining the polyurethane foam.
• a dehydrating agent (calcium oxide, calcium sulfide, calcium chloride, molecular sieve, etc.) may be added to the urethanization reaction component.
• the amount of dehydrating agent used is the sum of all components to obtain polyurethane foam It is preferably at most 8%, more preferably 0.5 to 6%, based on the mass.
• the prepolymer from (al) and (b) is used as a main component, and (a 2) is a catalyst, an antioxidant, etc.
• the above-mentioned polyurethane foam can be obtained by injecting both components into a mold with a two-component mixing casting machine using a premix of an additive and a foaming agent (for example, water) as a curing agent component.
• the above-mentioned prepolymer is used as a main component, and a premix of (a2) with a catalyst and an antioxidant is used as a hardener component.
• a premix of (a2) with a catalyst and an antioxidant is used as a hardener component.
• the t thin evening click ticks foam method above polyurethane foam is obtained for example, minutes main agent formed the above-described prepolymer, catalyst (a 2), oxide Sealant, as a curing agent component that combined pre mixing a dehydrating agent and hollow microspheres, and cast into a mold both components in two-liquid mixing casting machine, said polyurethane foam is obtained.
• the main agent component Isoshiane Ichito The equivalent ratio of the active hydrogen-containing group of the curing agent component to the group is preferably 0.7 to 1.5, more preferably 0.9 to 1.3.
• the content of urethane and Z or urea groups in the obtained polyurethane foam is preferably 0.5 to: L.8mo in order to obtain good mechanical properties before and after expansion.
• l Zl 000 g more preferably 0.6 to 1.5 mol Zl 00 00 g.
• the content of the aromatic ring in the polyurethane foam is preferably 0.1 to 1.5 mol 1 000 g in order to improve physical properties after water expansion. Omo l Z l OOO g is preferred.
• the content of the aromatic ring derived from the polyol in the polyurethane foam is preferably 0.1 to: 1.5 mol Zl 000 g, more preferably 0.15 to: L. 0 mo 1 Z 1 000 g. is there.
• the water-stopping material of the present invention comprises a molded or molded product of the above polyurethane foam.
• An example of the molding or forming method of the polyurethane foam is as follows. In a mold in which a cylindrical metal core is set at the center of a cylindrical mold, according to any of the foaming methods described above, the main component is used. And a curing agent component are cast, and preferably heat-cured at 60 to 150 ° C. for 2 to 30 hours to obtain a cylindrical molded article having a metal core at the center. This molded product is mounted on a band knife type milling machine usually used for producing a long sheet of a soft foam, and a sheet having a predetermined thickness is obtained.
• the foam sheet wound into a roll is cut into a predetermined width by a round knife cutter to obtain a band-shaped processed product of a polyurethane foam having a rectangular cross section.
• a polyurethane foam obtained by slab foaming without using a mold may be cut to obtain a molded product.
• a mixed liquid can be injected into a prismatic closed mold and cured by heating to produce a rod-shaped molded product.
• the water-stopping material of the present invention is formed by laminating a molded article or molded article of the polyurethane foam and a non-water-swellable porous or non-porous elastic body, for example, a laminated body as shown in FIG. It can also be.
• (1) is an oxyethylene group-containing polyurethane foam used in the present invention
• (2) is a non-water-swellable, porous or non-porous elastic material.
• the elastic body include those made of ordinary natural rubber or synthetic rubber (styrene rubber, butadiene rubber, isoprene rubber, chloroprene rubber, acrylonitrile-butadiene rubber, ethylene-propylene-gen rubber, butyl rubber, etc.).
• a porous elastic material can be used, and is preferably a non-water-swellable porous elastic material having a 50% compressive stress of 1 to 25 kgf / cm 2 similar to that of the above polyurethane foam.
• the water-stopping material of the present invention can be used as a normal segment sealing material or box culvert water-stopping material when the opening (gap) between segments is small during segment construction.
• FIG. 2 shows a perspective view of one embodiment of a segment with a tenon used in the shield d method when constructing a tunnel.
• FIG. 3 is a partial cross-sectional view showing a state in which a tenon (projection) and a tenon (recess) of the tenoned segment are combined to perform sealing.
• 21 is a tenon (convex)
• 22 is a tenon (recess)
• 23 and 24 are seal grooves
• 25 and 26 are seal grooves
• 27 is the space between rings.
• the fastening portion, 28 is the fastening portion between the pieces
• 30 is the waterproof material of the present invention.
• the direction of arrow A indicates the outward direction of the tunnel
• the direction of arrow B indicates the inward direction of the tunnel
• the surface indicated by arrow C is the surface of the tenon (recess side) of the tenoned segment.
• the surface indicated by the arrow D indicates the surface of the tenon (projection side) of the tenoned segment.
• a plurality of tenoned segments are prepared, and the tenon (concave side) of the side indicated by arrow C and the tenon (convex) on the side indicated by arrow D are prepared. Part), so that the tenon (projection) 21 and the tenon (recess) 22 fit respectively.
• the band-shaped water-stopping material 30 according to the present invention is inserted between the seal grooves 23 and 24 and between the seal grooves 25 and 26, respectively, for sealing.
• the seal grooves 25 and 26 do not exist depending on the shape of the segment. Will be introduced and sealed.
• the present invention will be further described with reference to examples, but the present invention is not limited to these examples.
• the main ingredient was the following prepolymer.
• the curing agent components were 1820 g of getyltoluenediamine, 27.1 g of water (foaming agent), 157 g of foam stabilizer "SZ-1931" (manufactured by Nippon Rikiichi Co., Ltd.) and 157 g of dibutyltin dilaurate. (Urethane-forming reaction catalyst) 15.7 g was mixed to prepare 2019.8 g.
• This molded product is cut into a sheet with a thickness of 10 mm using a pilling machine, wound up in a roll shape, and then cut into a 20 mm width by a round knife cutter.
• a strip-shaped molded product having a width of 10 mm and a width of 20 mm was obtained. Table 1 shows the characteristic values of this band-shaped molded product.
• the main ingredient was the following prepolymer.
• the curing agent component was E-adduct of bisphenol A (number average molecular weight: 670) 5380 g, foam stabilizer "SZ-1931" (Nippon Rikiichi Co., Ltd.) 157 g, octyl 5.89.7 g was prepared by mixing 53.7 g of lead acid (a urethanization reaction catalyst) and 269 g of "Molecular Sieve 3 AB" (a dehydrating agent) (manufactured by Union Carbide Co., Ltd.).
• the main component and the curing agent component are dried at the above liquid ratio (the ratio of the equivalent ratio of hydroxyl group to the isocyanate group of prepolymer is 1.03) at a speed of 3 k in total for 0.8 liter.
• the main agent was "Duranate D-101" [manufactured by Asahi Kasei Kogyo Co., Ltd., hydrogenated MDI bifunctional prepolymer, isocyanate group content 19.0% by mass] 1653 g.
• the curing agent component is 4000 g of polyether glycol with a number average molecular weight of 4,000 obtained by adding a mixture of E ⁇ and PO (mass ratio 80/20) to bisphenol A, and a mixture of EO and P ⁇ in glycerin. (Mass ratio 20Z80) to a mixture of 6000 g of polyether triol having a number average molecular weight of 300,000 obtained by adding a foam stabilizer “SZ—1931” [Nihonika
• the main agent and the curing agent component were mixed at a rate of 3 kgZ in a total of 3 kgZ at the above liquid ratio (the ratio of the hydroxyl group to the isocyanate group of "Duranate D-101" being 1.10).
• Table 1 shows the characteristic values of this band-shaped molded product.
• Example 4 When the cylindrical molded product having a metal core in the center obtained in Example 1 was cut into a sheet having a thickness of 7 mm using a peeling machine and wound into a roll, A 3 mm thick black mouth plain foam (containing closed cells, density 0.85 gZcm 3 , compressive stress at a compressibility of 50%: 20 kgf Zcm 2 ) is applied to a black mouth plain adhesive ("Quick Dry Pond G-1 7 ": manufactured by Konishi Co., Ltd.), and wound into a roll while being bonded, and cut into 20 mm-wide strips to obtain a strip-shaped molded product having a thickness of 10 mm and a width of 20 mm. Table 1 shows the characteristic values of this band-shaped molded product.
• polyacrylate-based water-absorbent resin "Sanfresh ST-500MPS” manufactured by Sanyo Chemical Industries, Ltd.
• isobutylene-maleic anhydride alternating copolymer-based water-absorbent resin "KI” Gel 20 1K-F2 "[Kuraray Co., Ltd.] was kneaded with the following composition (parts by mass) as a water-absorbing resin, and then vulcanized and foamed at 150 for 30 minutes, cooled, and cooled. A part of the bubbles was broken by the pressure to obtain a water-swellable rubber foam of half-semi-solo (closed cell content: 50%). This was cut into a strip having a thickness of 10 mm and a width of 20 mm to obtain a specimen.
• TD I-65 As a main agent, 30.8 parts by mass of TD I-65 was used.
• the curing agent component is "EP-550H” (polyether polyol containing no oxyethylene group, manufactured by Mitsui Nisso Co., Ltd.) 100 parts by mass of "SUMIGA GEL A-40” (water-absorbent resin) [Sumitomo Chemical Co., Ltd.), foam stabilizer "F-258” [Shin-Etsu Chemical Co., Ltd.] 2 parts by mass, suinosuccitoate (urethanization reaction catalyst) 0.15 parts by mass and water (foaming agent) 0.5 parts by mass were mixed.
• Example 1 In the same manner as in Example 1, the main agent and the curing agent component were mixed and cast at the above-mentioned liquid ratio (a ratio at which the equivalent ratio of the hydroxyl group to the isocyanate group of TDI-65 was 1.20). Heat cured at 10 for 3 hours, cured at 24 at 80 for 24 hours, peeled to a thickness of 10 mm, and cut to a width of 20 mm to obtain a strip-shaped processed product with a thickness of 10 mm and a width of 20 mm . This was pressurized to break some of the bubbles to obtain a water-swellable rubber foam of semi-semi-solo (closed cell content 50%). Table 1 shows the characteristic values of this band-shaped molded product.
• Table 2 shows the tensile properties of each of the specimens of Examples 1-4 and Comparative Examples 1 and 2
• Table 3 shows the results of the long-term expansion test and mass reduction test
• Table 4 shows the results of the stress relaxation test
• Table 5 shows the results of the water performance test. The test method is as follows.
• a 20 x 20 x 2 mm test piece was sampled from the sample strip, and the volume of this test piece when immersed in the purified water in step 23 was measured every day. The magnification was calculated, and the magnification when the amount of increase in volume per day became 0.01 or less was defined as the volume expansion ratio of the test piece.
• Volume expansion ratio (times) Volume after expansion Z Volume before expansion
• test piece A 20 ⁇ 20 ⁇ 2 mm test piece was collected from the sample strip, and the volume of this test piece immersed in 23 T purified water was measured at predetermined intervals and calculated by the following formula. .
• volume expansion rate (%) 100 x (volume after expansion-volume before expansion) Volume before expansion
• a specimen of 20 ⁇ 20 ⁇ 2 mm was taken from the sample strip, and the specimen was immersed in purified water at 70 for 7 days, and then dried in an oven at 60, The mass when the decrease in mass became 0.1 g or less was defined as the mass after drying, and was calculated by the following equation.
• Mass reduction rate (%) 100 X (mass before expansion-mass after drying) (Mass loss rate [23t:])
• the test piece after the swelling coefficient was measured for 180 days was dried in an oven at 60.
• the mass when the decrease in mass was 0.1 g or less was calculated as the mass after drying according to the following equation.
• Mass reduction rate (%) 100 X (mass before expansion-mass after drying) Mass before expansion
• a test piece of 10 cm of the waterproof material of Examples 1 to 4 and Comparative Examples 1 and 2 was sandwiched between a pair of two steel flat plates, and compressed to a compression ratio of 50% by a compression tester. Then, the change with time of the compressive stress was measured, and the retention rate of the compressive stress before the relaxation was started was calculated.
• test pieces (5) of the waterproof material of Examples 1 to 4 and Comparative Examples 1 and 2 were placed on the lower plate surface of a pair of steel flanges (3 and 4).
• FIG. 5 indicates an air vent valve.
• the water-stopping material of the present invention is a water-stopping material comprising a molded article or a molded article of an oxyethylene group-containing polyurethane foam. Since the swelling itself expands, it does not contain swelling components that elute into water, has a low mass reduction rate, and exhibits stable swelling performance over a long period of time.
• the waterproof material of the present invention can be used as a normal seal material for a segment or a waterproof material for a box culvert when the opening (gap) between the segments is small at the time of segment construction.
• the combination surface of the segments has irregularities, and a lower compressive stress is required for the fitting. is there.

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• 1999
  • 1999-07-07 WO PCT/JP1999/003686 patent/WO2000002973A1/ja active IP Right Grant
  • 1999-07-07 DE DE69912467T patent/DE69912467T2/de not_active Expired - Fee Related
  • 1999-07-07 EP EP99929748A patent/EP1116766B1/de not_active Expired - Lifetime

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